MiR-34a-5p promotes autophagy and apoptosis of ovarian granulosa cells via the Hippo-YAP signaling pathway by targeting LEF1 in chicken

Poult Sci. 2023 Feb;102(2):102374. doi: 10.1016/j.psj.2022.102374. Epub 2022 Dec 5.

Abstract

Follicular atresia is a natural physiological phenomenon in poultry reproduction. It is well known that follicular atresia is caused by both autophagy and apoptosis of granulosa cells. In current experiment, we evaluated the function of miR-34a-5p on autophagy and apoptosis in chicken follicular atresia. First, the follicular atresia model of chicken was successfully constructed by subcutaneous injection of tamoxifen (TMX), and found the expression of miR-34a-5p in the atresia follicles obviously increased. Then, we confirmed that miR-34a-5p accelerates autophagy and apoptosis of chicken granulose cells in vitro, and miR-34a-5p could induce apoptosis by mediating autophagy. Mechanistically, lymphoid enhancer binding factor 1 (LEF1) was deemed as a target gene for miR-34a-5p. On the contrary, LEF1 overexpression attenuated the autophagy and apoptosis of chicken granular cells. In addition, it was confirmed that the miR-34a-5p/LEF1 axis plays a regulatory role in chicken granulosa cells by mediating the Hippo-YAP signaling pathway. Taken together, this study demonstrated that miR-34a-5p contributes to autophagy and apoptosis of chicken follicular granulosa cells by targeting LEF1 to mediate the Hippo-YAP signaling pathway.

Keywords: Hippo-YAP pathway; LEF1; apoptosis; autophagy; miR-34a-5p.

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Autophagy / physiology
  • Cell Proliferation / genetics
  • Chickens / genetics
  • Chickens / metabolism
  • Female
  • Follicular Atresia
  • Granulosa Cells / metabolism
  • Hippo Signaling Pathway
  • Lymphoid Enhancer-Binding Factor 1 / genetics
  • Lymphoid Enhancer-Binding Factor 1 / metabolism
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • YAP-Signaling Proteins / metabolism

Substances

  • Lymphoid Enhancer-Binding Factor 1
  • MicroRNAs
  • YAP-Signaling Proteins